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. 2019 Mar 22;10(2):132–140. doi: 10.1016/j.jtcme.2019.03.006

Fig. 4.

Fig. 4

Effects of M. alba stem extract (MSE), oxyresveratrol (OXY), glucosamine sulfate (GS) and diclofenac sodium (DCS) on IL-1β-induced PGE2 production (A) and COX-2 protein expression (B) in the C28/I2 human chondrocyte cell line. The cells were untreated (Bar 1), only stimulated with IL-1β 10 ng/mL (Bar 2) and pretreated with various concentrations of MSE and OXY as well as GS 10 μg/mL and DCS 10 μg/mL for 2 h and then stimulated by 10 ng/mL IL-1β for 22 h. The cell culture supernatant was collected and determined the PGE2 production by using ELISA kit. The concentration of PGE2 was normalized to the activated control. The expression of COX-2 (72 kDa) was determined by western blotting analysis and GAPDH protein (38 kDa) was used as a loading control. The data are expressed as mean ± S.D. of three independent experiments. **p < 0.01 compared to the IL-1β-stimulated cells.